HCID 44137409, compound → HCID 44196880, compound

HRID 1919863Notes

Reaction equation

HRID 1919863 reaction equation
C([O:3][C:4](=[O:33])[CH2:5][N:6]1[C:14]2[C:9](=[CH:10][C:11]([F:15])=[CH:12][CH:13]=2)[C:8]([CH2:16][C:17]2[CH:22]=[CH:21][C:20]([S:23]([CH:26]3[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]3)(=[O:25])=[O:24])=[CH:19][CH:18]=2)=[C:7]1[CH3:32])C.C1(S(C2C=CC=CC=2CC2C3C(=CC=C(F)C=3)N(CC(O)=O)C=2C)(=O)=O)CCCCC1>>[CH:26]1([S:23]([C:20]2[CH:19]=[CH:18][C:17]([CH2:16][C:8]3[C:9]4[C:14](=[CH:13][CH:12]=[C:11]([F:15])[CH:10]=4)[N:6]([CH2:5][C:4]([OH:33])=[O:3])[C:7]=3[CH3:32])=[CH:22][CH:21]=2)(=[O:24])=[O:25])[CH2:27][CH2:28][CH2:29][CH2:30][CH2:31]1

Participants

3

Reactant 2

HCID 44137409HCID 44137409, compoundHCID 67490739HCID 67490739, compound

Product 1

HCID 44196880HCID 44196880, compound

Procedure

2-(3-(4-(Cyclohexylsulfonyl)benzyl)-5-fluoro-2-methyl-1H-indol-1-yl)acetic acid ethyl ester was used as the starting material, otherwise this compound was prepared in a similar manner to Compound 1, using Procedure L.

Sources & evidence

ORD record
ord-1472e56ca7de4e0a8c38d604f2b41726
Source dataset
uspto-grants-2012_05
Patent number
US08168673B2

Reaction notes

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